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1-Butanethiol (CAS 109-79-5)

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Alternate Names:
Butyl mercaptan; Mercaptan C4; butane-1-thiol
Application:
1-Butanethiol is used as a model gaseous analyte for fast-responding membrane-free amperometric gas sensor
CAS Number:
109-79-5
Molecular Weight:
90.19
Molecular Formula:
C4H10S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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1-Butanethiol is a chemical compound that functions as a reagent in organic synthesis. It acts as a nucleophile in thiol-disulfide exchange reactions, facilitating the formation of carbon-sulfur bonds. 1-Butanethiol′s mechanism of action involves its ability to undergo substitution reactions with electrophiles, leading to the introduction of a thiol group into organic molecules. In experimental applications, 1-butanethiol is utilized to modify 1-Butanethiol properties of target compounds, allowing for the synthesis of new materials or the functionalization of existing molecules. its reactivity as a sulfur-containing compound, enabling the creation of diverse chemical structures through thiol chemistry. 1-Butanethiol′s mechanism of action at the molecular level involves its interaction with other functional groups, leading to the formation of thioethers and other sulfur-containing derivatives. 1-butanethiol serves as a versatile building block in organic synthesis, contributing to the development of novel compounds and materials.


1-Butanethiol (CAS 109-79-5) References

  1. On-column derivatization-capillary electrochromatography with o-phthalaldehyde/alkylthiol for assay of biogenic amines.  |  Oguri, S., et al. 2004. J Chromatogr A. 1044: 271-6. PMID: 15354448
  2. Conformationally specific vacuum ultraviolet mass-analyzed threshold ionization spectroscopy of alkanethiols: structure and ionization of conformational isomers of ethanethiol, isopropanethiol, 1-propanethiol, tert-butanethiol, and 1-butanethiol.  |  Choi, S., et al. 2008. J Phys Chem A. 112: 7191-9. PMID: 18636705
  3. Stability of volatile sulfur compounds (VSCs) in sampling bags - impact of temperature.  |  Le, H., et al. 2013. Water Sci Technol. 68: 1880-7. PMID: 24185074
  4. Probing the molecular forces involved in binding of selected volatile flavour compounds to salt-extracted pea proteins.  |  Wang, K. and Arntfield, SD. 2016. Food Chem. 211: 235-42. PMID: 27283627
  5. Effect of Selected Mercapto Flavor Compounds on Acrylamide Elimination in a Model System.  |  Xiong, Z., et al. 2017. Molecules. 22: PMID: 28561777
  6. It's a Trap: Thiol-Michael Chemistry on a DASA Photoswitch.  |  Alves, J., et al. 2020. Chemistry. 26: 809-813. PMID: 31797435
  7. Efficient tandem solar cells with solution-processed perovskite on textured crystalline silicon.  |  Hou, Y., et al. 2020. Science. 367: 1135-1140. PMID: 32139544
  8. Changes of Exhaled Volatile Organic Compounds in Postoperative Patients Undergoing Analgesic Treatment: A Prospective Observational Study.  |  Löser, B., et al. 2020. Metabolites. 10: PMID: 32784730
  9. Conformations and Low-Frequency Intramolecular Motions of 1-Butanol, 1-Butanethiol, Iso-butanol, and Iso-butanethiol Investigated by Fourier Transform Microwave Spectroscopy Combined with Quantum Chemical Calculations.  |  Kawashima, Y., et al. 2021. J Phys Chem A. 125: 1166-1183. PMID: 33502865
  10. Localized surface plasmon resonance inflection points for improved detection of chemisorption of 1-alkanethiols under total internal reflection scattering microscopy.  |  Ryu, KR., et al. 2021. Sci Rep. 11: 12902. PMID: 34145319
  11. Adsorption performance and mechanisms of mercaptans removal from gasoline oil using core-shell AC-based adsorbents.  |  Ndagijimana, P., et al. 2021. Environ Sci Pollut Res Int. 28: 67120-67136. PMID: 34245419
  12. Characterization of volatile thiols in Chinese liquor (Baijiu) by ultraperformance liquid chromatography-mass spectrometry and ultraperformance liquid chromatography-quadrupole-time-of-flight mass spectrometry.  |  Yan, Y., et al. 2022. Front Nutr. 9: 1022600. PMID: 36263305
  13. Reactions of mercaptans with cytochrome c oxidase and cytochrome c.  |  Wilms, J., et al. 1980. Biochim Biophys Acta. 589: 324-35. PMID: 6243968

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1-Butanethiol, 250 ml

sc-396834
250 ml
$61.00